Planet Pharma
The research we do and the products we develop improve outcomes for patients around the world. As an Associate Scientist I at , your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. As a key part of projects, our research and development team is responsible for delivering results to drive decisions and ensure safety of our existing and new products. We work on products that make a meaningful difference in others’ lives. When you join you’ll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure!
Responsibilities:
Conduct critical chemical and physical analyses on finished product R&D stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives. Work under minimum supervision
Perform chemical assays requiring precise analytical skills and understanding of chemistry principles
Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations
Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support
Use sophisticated laboratory instrumentation (HPLC, pH, UV, titrations, Particle, TOC, Flame photometry, etc) and computer systems to collect and record data.
Follow, understand and comply with SOPs and policies on cGMPs and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas
Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation.
Required:
Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences, biology) 6 months or more of experience
Analytical chemistry instrumentation experience with HPLC, pH, UV, titrations, Particle, TOC is preferred but not required
Must have experience in a regulated environment and strong technical problem-solving skills
Must have good oral and written communication skills, strong analytical skills and be detail oriented
Electronic Lab Notebook experience is preferred but not required
Pharmaceutical GMP laboratory experience is desired
Empower experience is preferred
Must be able to handle multiple tasks concurrently and in a timely fashion.
Possess relevant laboratory/technical, writing, and computer skills
Ability to organize and communicate complex information effectively with managers and peers
Physical Activities and Requirements:
Must be able to hand write and use computers for the majority of the work day
Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing
May require standing for extended periods
Must be able to lift up to 10 pounds routinely
Must not be color blind
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Responsibilities:
Conduct critical chemical and physical analyses on finished product R&D stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives. Work under minimum supervision
Perform chemical assays requiring precise analytical skills and understanding of chemistry principles
Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations
Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support
Use sophisticated laboratory instrumentation (HPLC, pH, UV, titrations, Particle, TOC, Flame photometry, etc) and computer systems to collect and record data.
Follow, understand and comply with SOPs and policies on cGMPs and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas
Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation.
Required:
Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences, biology) 6 months or more of experience
Analytical chemistry instrumentation experience with HPLC, pH, UV, titrations, Particle, TOC is preferred but not required
Must have experience in a regulated environment and strong technical problem-solving skills
Must have good oral and written communication skills, strong analytical skills and be detail oriented
Electronic Lab Notebook experience is preferred but not required
Pharmaceutical GMP laboratory experience is desired
Empower experience is preferred
Must be able to handle multiple tasks concurrently and in a timely fashion.
Possess relevant laboratory/technical, writing, and computer skills
Ability to organize and communicate complex information effectively with managers and peers
Physical Activities and Requirements:
Must be able to hand write and use computers for the majority of the work day
Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing
May require standing for extended periods
Must be able to lift up to 10 pounds routinely
Must not be color blind
#J-18808-Ljbffr